2-Imidazoline synthesis

Molbank

Following our interest in synthesis and chemistry of 1 2-diamines [29 30 31] herein we report the synthesis of previously unknown 1-benzyl-2-(thien-2-yl)-4 5-dihydro-1 H-imidazole through a slightly modified Fujioka's procedure giving the title compound in a good 78% yield

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2

Description: 2-Methylthio-2-imidazoline hydriodide is only for laboratory use 2-Methylthio-2-imidazoline hydriodide can also be found under its synonyms cas or the MDL number For the COA of cas or the MSDS sheet please send an inquiry via email This chemical structure has a Molecular weight of 244 09 and chemical formula is C4H8N2S HI

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2

2-Phenyl-2-imidazoline (936-49-2) is used as a pharmaceutical raw materials or used in organic synthesis epoxy powder coating curing agent 2-PHENYL-2-IMIDAZOLINE Toxicity Data With Reference 1 ivn-uns LDLo:67 mg/kg : AEPPAE Naunyn-Schmiedeberg's Archiv fuer Experimentelle Pathologie und Pharmakologie 192 (1939) 141 2-PHENYL-2-IMIDAZOLINE Consensus Reports

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The Existence of Imidazoline Corrosion Inhibitors

Within a 20 day interval after inhibitor synthesis this ratio decreased by a factor greater than 20 These results as well as a discussion of their economic impact on oilfield corrosion inhibitor formulation are presented in this paper Cited by Adnan Munis Tianyu Zhao Maosheng Zheng Ata Ur Rehman and Feng Wang (2020) A newly synthesized green corrosion inhibitor imidazoline derivative

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2

Synonym: 2-Benzyl-2-imidazoline 2-Benzyl-4 5-dihydro-1H-imidazole Benzidazol NSC 35110 Phenylmethylimidazoline Tolazoline CAS Number 59-98-3 Empirical Formula (Hill Notation) C 10 H 12 N 2 Molecular Weight 160 22 EC Number 200-448-9 MDL number MFCD00005182 PubChem Substance ID 24857660 NACRES NA 22

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2

2-Phenyl-2-imidazoline pyromellitate (CAS No : 54553-90-1) is our strong product We have bulk quantity in stock usually and our price is very competitive Please email us for more detailed information and updated quotation for our 2-Phenyl-2-imidazoline pyromellitate (CAS No : 54553-90-1) ‍

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Potent orally available selective COX

A novel series of compounds containing a polar non-flat 2-imidazoline core was designed based on the SAR information available for aromatic azole cyclooxygenase-2 inhibitors While the majority of the compounds prepared using an earlier developed imidazoline N-arylation methodology turned out to be inferior to the known COX-2 inhibitors one lead compound displayed potency (300 nM) comparable

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Buy 1

Chiral Synthesis Tools Molarity Calculator Molecular Weight Calculator Periodic Table About us View more Advantages Inhibitors 1-Methyl-2-(2-thymoxymethyl)-2-imidazoline hydrochloride * For research use only Not for human or veterinary use CAS No : 101564-98-1 Main Products Catalog No : VC016677 Molecular Formula: C15H22N2O ClH Molecular Weight: 282 813 Product Introduction

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Synthesis of 2 6

Synthesis of 2 6-Di(2'-imidazoline-2'-yl)Pyridine under Microwave Irradiation and Interaction with DNA ZHANG Jin-Yan 1 XIAO Xiao-Ming 1 * TAN Nian-Yuan 2 XU Sha-Sha 1 OUYANG Ze-Ying 1 (1 College of Chemistry and Chemical Engineering Hunan Normal University Changsha 410081 2 College of Chemistry and Chemical Engineering Hunan Institute of Engineering Xiangtan) Abstract Related

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Imidazoline

Imidazoline is a class of heterocycles formally derived from imidazoles by the reduction of one of the two double bonds Three isomers are known 2-imidazolines 3-imidazolines and 4-imidazolines The 2- and 3-imidazolines contain an imine center whereas the 4-imidazolines contain an alkene group The 2-Imidazoline group occurs in several drugs

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2

Categories: Synthesis of N-Heterocycles Synthesis of 2-imidazolines Recent Literature An efficient preparation of 2-imidazolines was achieved from aldehydes and ethylenediamines in the presence of tert-butyl hypochlorite By this method 1 3-bis(imidazolin-2-yl)benzene and 2 6-bis(imidazolin-2-yl)pyridine which act as chiral ligands could be prepared directly from the corresponding

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Palladium

We describe the palladium-catalyzed multicomponent synthesis of 2-imidazolines This reaction proceeds via the coupling of imines acid chlorides and carbon monoxide to form imidazolinium carboxylates followed by a decarboxylation Decarboxylation in CHCl3 is found to result in a mixture of imidazolinium and imidazolium salts However the addition of benzoic acid suppresses aromatization

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2

2-Methyl-2-imidazoline supply Structure Search Substructure Search Similarity Search Home Product Listing Enquiries: infoamerican-chemicals Chemical Name CAS Structure Search This Request For Quotation will be sent to the supplier directly The supplier shall contact you shortly Supplier: Chemical Name: 2-Methyl-2-imidazoline CAS: 534-26-9 Quantity Required: * Company Name

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2

Description: 2-Methylthio-2-imidazoline hydriodide is only for laboratory use 2-Methylthio-2-imidazoline hydriodide can also be found under its synonyms cas or the MDL number For the COA of cas or the MSDS sheet please send an inquiry via email This chemical structure has a Molecular weight of 244 09 and chemical formula is C4H8N2S HI

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2

Kinetics of the reaction of 2-methyl-2-imidazoline with sulfate and hydrogen phosphate radicals has been investigated by flash-photolysis Rate constant for the reaction was reported to be 10 8-10 9 M-1 s-1 Application 2-Methyl-2-imidazoline may be used in the synthesis of series of N N N′-trisubstituted ethylenediamine derivatives

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2

2-Methylthio-2-imidazoline hydriodide is a reactant for synthesis of: aurora and epidermal growth factor receptor kinase inhibitors spiro-piperidine inhibitors galegine analogues guanidinyl pyrrolidines as bifunctional catalysts carbonic anhydrase inhibitors and small molecule CXCR4 antagonists

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Synthesis of 2 6

Synthesis of 2 6-Di(2'-imidazoline-2'-yl)Pyridine under Microwave Irradiation and Interaction with DNA ZHANG Jin-Yana XIAO Xiao-Minga TAN Nian-Yuanb XU Sha-Shaa OUYANG Ze-Yinga(aCollege of Chemistry and Chemical Engineering Hunan Normal University Changsha 410081 bCollege of Chemistry and Chemical Engineering Hunan Institute of Engineering Xiangtan) 2 6-Di(2'-imidazoline-2'

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